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rs7090512

From SNPedia

Orientationplus
Stabilizedplus
Make rs7090512(C;C)
Make rs7090512(C;T)
Make rs7090512(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position6068866
is asnp
is mentioned by
dbSNPrs7090512
ebirs7090512
HLIrs7090512
Exacrs7090512
Varsomers7090512
Maprs7090512
PheGenIrs7090512
hapmaprs7090512
1000 genomesrs7090512
hgdprs7090512
ensemblrs7090512
gopubmedrs7090512
geneviewrs7090512
scholarrs7090512
googlers7090512
pharmgkbrs7090512
gwascentralrs7090512
openSNPrs7090512
23andMers7090512
23andMe allrs7090512
SNP Nexus

SNPshotrs7090512
SNPdbers7090512
MSV3drs7090512
GWAS Ctlgrs7090512
GMAF0.3471
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele G
P-val 5E-20
Odds Ratio 1.1900 [1.17-1.21]

[PMID 19956101OA-icon.png] Overview of the Rapid Response data.


[PMID 24332945] Interleukin 2 receptor α chain gene polymorphisms and risks of multiple sclerosis and neuromyelitis optica in southern Japanese